<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Linden M</submitter><funding>Vetenskapsrådet</funding><funding>•the Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement</funding><funding>Barncancerfonden</funding><funding>Cancerfonden</funding><pagination>107</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12455829</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>FET (FUS, EWSR1, and TAF15) fusion oncoproteins are characteristic for several sarcomas and leukemias, including myxoid liposarcoma and Ewing sarcoma. FET oncoproteins interact with the SWI/SNF chromatin remodeling complex subtypes cBAF, PBAF, and GBAF, but their impact on SWI/SNF compositions, interactions, and downstream epigenetic effects remains elusive.&lt;h4>Methods&lt;/h4>We employ a comprehensive immunoprecipitation and quantitative mass spectrometry approach to determine the impact of FET oncoproteins on SWI/SNF composition and their interactomes. Validation of complex composition and interaction partners is performed by glycerol gradient sedimentation assays and co-immunofluorescence analysis. Furthermore, we determine the differential chromatin accessibility and gen</pubmed_abstract><journal>Cellular &amp; molecular biology letters</journal><pubmed_title>FET fusion oncoproteins enrich SWI/SNF complex subtypes and interaction partners.</pubmed_title><pmcid>PMC12455829</pmcid><funding_grant_id>965065</funding_grant_id><funding_grant_id>22-2470</funding_grant_id><funding_grant_id>1006009</funding_grant_id><funding_grant_id>2023-02239</funding_grant_id><funding_grant_id>966318</funding_grant_id><funding_grant_id>22-2080</funding_grant_id><funding_grant_id>2021-01008</funding_grant_id><funding_grant_id>D2025-0003</funding_grant_id><funding_grant_id>2022-0030</funding_grant_id><pubmed_authors>Andersson L</pubmed_authors><pubmed_authors>Aman P</pubmed_authors><pubmed_authors>Sjovall D</pubmed_authors><pubmed_authors>Jaako P</pubmed_authors><pubmed_authors>Linden M</pubmed_authors><pubmed_authors>Jonasson E</pubmed_authors><pubmed_authors>Crescitelli R</pubmed_authors><pubmed_authors>Fagman H</pubmed_authors><pubmed_authors>Stahlberg A</pubmed_authors><pubmed_authors>Albatrok H</pubmed_authors><pubmed_authors>Canfjorden V</pubmed_authors><pubmed_authors>Gronqvist K</pubmed_authors></additional><is_claimable>false</is_claimable><name>FET fusion oncoproteins enrich SWI/SNF complex subtypes and interaction partners.</name><description>&lt;h4>Background&lt;/h4>FET (FUS, EWSR1, and TAF15) fusion oncoproteins are characteristic for several sarcomas and leukemias, including myxoid liposarcoma and Ewing sarcoma. FET oncoproteins interact with the SWI/SNF chromatin remodeling complex subtypes cBAF, PBAF, and GBAF, but their impact on SWI/SNF compositions, interactions, and downstream epigenetic effects remains elusive.&lt;h4>Methods&lt;/h4>We employ a comprehensive immunoprecipitation and quantitative mass spectrometry approach to determine the impact of FET oncoproteins on SWI/SNF composition and their interactomes. Validation of complex composition and interaction partners is performed by glycerol gradient sedimentation assays and co-immunofluorescence analysis. Furthermore, we determine the differential chromatin accessibility and gen</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T19:38:59.684Z</modification><creation>2026-04-30T03:12:31.648Z</creation></dates><accession>S-EPMC12455829</accession><cross_references><pubmed>40988026</pubmed><doi>10.1186/s11658-025-00792-w</doi></cross_references></HashMap>